Table 3.
Clinical trials evaluating beta-blockers for the preventing anthracycline-induced cardiotoxicity.
| Therapies | Cancer | Trial design | Follow up | Results | Ref. |
|---|---|---|---|---|---|
| Carvedilol or placebo | Breast cancer | Prospective, randomized, double-blind, placebo-controlled (n = 200) | 6 months | No differences in changes of LVEF or B-type natriuretic peptide were noted between groups. A significant difference existed between groups in troponin I levels, with lower levels in the carvedilol group. Additionally, a lower incidence of diastolic dysfunction was noted in the carvedilol group | Avila et al. (130) |
| Placebo vs. candesartan vs. metoprolol vs. candesartan + metoprolol | Breast cancer | 2 × 2 factorial, randomized, placebo-controlled, double-blind trial (n = 130) | 3–5 months | No significant effect on change in LVEF with metoprolol vs. Placebo | Gulati et al. (123) |
| Carvedilol vs. placebo | Breast cancer | Double-blind randomized trial (n = 70) | 1 week | No significant reduction in strain and strain-rate parameters upon intervention, but an obvious decrease in these parameters was observed in the placebo arm | Tashakori Beheshti et al. (133) |
| Carvedilol vs. placebo | Breast cancer | Randomized, single-blind, placebo-controlled (n = 91) | 6 months | LVEF did not alter in the carvedilol arm (from 58.7% to 57.4%), but remarkably decreased in the placebo arm (from 61.1% to 51.6%) | Nabati et al. (129) |
| Carvedilol [6.25 mg/day (n = 41), 12.5 mg/day (n = 38) or 25 mg/day (n = 37)] vs. placebo (n = 38) | Various cancers | Prospective, randomized, double-blind (n = 154) | 6 months | LVEF reduced from 62 ± 5% to 58 ± 7% at 6 months in the control arm, however no significant alterations occurred in the 3 carvedilol arms | Abuosa et al. (134) |